{"data":{"id":"us/21-cfr-607.21","jurisdiction":"us","citation":"21 CFR 607.21","heading":"Times for establishment registration and blood product listing.","body":"The owner or operator of an establishment entering into an operation defined in § 607.3(d) shall register such establishment within 5 days after the beginning of such operation and submit a list of every blood product in commercial distribution at the time. If the owner or operator of the establishment has not previously entered into such operation (defined in § 607.3(d) of this chapter) for which a license is required, registration shall follow within 5 days after the submission of a biologics license application in order to manufacture blood products. Owners or operators of all establishments so engaged must register annually between October 1 and December 31 and must update their blood product listing every June and December.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER F—BIOLOGICS","PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES","Subpart B—Procedures for Domestic Blood Product Establishments"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"30f56658615af9d4f570779c982c8db3200f13c9b1f5430f41cb711b80e82770","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-607.20","next":"us/21-cfr-607.22"},"notice":"GroundRules: Original legal text. Not legal advice."}